The Clinical Studies Center provides:
-
Qualified and Experienced Administrative Support
- Training and Education for Research
Staff
- Assistance with Protocol Submissions
- Reception Area
- Fully-Equipped Exam & Interview Rooms for Research
Visits
- Fully-Equipped Laboratory for Specimen Handling,
Storage, and Shipping
- Work Area Designated for Sponsors'
Representative Visits
- Daily Pick-Up for Federal Express
and DHL/Airborne Express
The Office
of Human Research Protection (OHRP) provides
guidance and regulations in human research.
The Food
and Drug Administration (FDA) provides biologic/device
guidance and regulations.
The University
of Michigan School of Medicine provides
a copy of the Code Of Federal Regulation 45CFR50:
Protection of
Human
Subjects.
Explore the Association
of Clinical Research Professionals (ACRP) website
and learn about the many membership benefits and educational
opportunities offered. This site also
contains information on ACRP publications, their leadership,
and how to join research professionals worldwide who
have already become ACRP members.
The Society
of Clinical Research Associates (SoCRA),
Inc., is a non-profit, professional organization dedicated
to the continuing education and development of clinical
research professionals. The
organization has also established and maintains
an international certification
program for clinical research professionals.
Public Responsibility
in Medicine and Research (PRIM&R) has
been committed to the advancement of strong research
programs and to the consistent application of ethical
precepts in both medicine and research. Through national
conferences and published reports thereon, it has addressed
a broad range of issues in biomedical and behavioral
research, clinical practice, ethics, and the law.
The
Emory University School of Medicine Clinical Trials
Office exists to ensure leading-edge, efficient clinical
trial investigations, yielding improved patient care
and outcomes. The mission of the CTO is to organize and
enhance operational processes that support clinical trial
efforts of Investigators
and facilitate the timely initiation, execution, management
and completion of clinical trials, guided by the highest
ethical and research standards.